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Circulating Factors in Nephrotic Syndrome

Circulating Factors in Nephrotic Syndrome - A Prospective Observational Cohort Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06315504
Enrollment
104
Registered
2024-03-18
Start date
2024-04-01
Completion date
2034-04-01
Last updated
2024-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Membranous Nephropathy, Minimal Change Disease, Nephrotic Syndrome, Primary Focal Segmental Glomerulosclerosis

Brief summary

A prospective observational study to investigate the treatment-associated changes of circulating factors associated with glomerular diseases among patients with de novo nephrotic syndrome admitted to hospital for a kidney biopsy.

Interventions

OTHERObservation

Observation

Sponsors

Iain Bressendorff
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age ≥ 18 years * Plasma albumin \< 36 g/L * Urine protein \>3.5 g/day or urine protein/creatinine-ratio (UPCR) \> 3.5 or urine albumin/creatinine-ratio (UACR) \>2200 mg/g * Planned kidney biopsy * Able to give written informed consent

Exclusion criteria

* Kidney transplant recipient * Previously undergone a kidney biopsy * Unable to understand written information in Danish

Design outcomes

Primary

MeasureTime frameDescription
levels of anti-nephrin in blood by ELISAup to 12 monthstemporal association of anti-nephrin with clinical remission of nephrotic syndrome

Secondary

MeasureTime frameDescription
changes in auto-antibodies in blood associated with membranous nephropathyup to 24 monthstemporal association of auto-antibodies with clinical remission of nephrotic syndrome

Contacts

Primary ContactIain Bressendorff, MD PhD
iain.oshoej.bressendorff@regionh.dk+4524277139
Backup ContactDitte Hansen, MD PhD
ditte.hansen.04@regionh.dk+4538682056

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026